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Clinical Research Associate (CRA) St Petersburg DOKUMEDS St Petersburg

Clinical Research Associate (CRA) St Petersburg

St Petersburg
2020-11-18 10:15:56
Clinical Research Associate (CRA) St Petersburg
Clinical Research Associate (CRA) Dokumeds is European focused CRO, with registered offices across Europe and trusted partners around the world. Our team of highly trained and dedicated professionals having significant role to ensure the conduct of international clinical studies in adherence to highest standards and regulatory requirements across the Europe and many other countries. We truly believe that a company can only be as good as the people behind it. Therefore, we believe in employing individuals who are not only professionals in their field, but also who are full of initiative and passionate about what they do. Dokumeds staff actively take part in cross-functional projects and their day is never limited to just the standard job description. They are self-motivated, willing to learn and share their knowledge with others. They are customer and result-oriented, open communicators and always willing to develop themselves and the business. Dokumeds is looking for highly motivated... and proactive clinical research professional willing to develop together with the company in position of Clinical Research Associate (CRA) located in Russia: CRA is responsible for all aspects of study site management including site selection, initiation, routine monitoring, close-out and maintenance of study files. CRA also ensures the quality and integrity of data, compliance with relevant SOPs and regulatory requirements and study completion on time and within budget. Job Responsibilities: Site administration and site monitoring responsibility for assigned clinical studies according to Dokumeds and Sponsor Standard Operating Procedures, legal requirements and ICH-GCP Guidelines Conduct of country and site feasibility Site selection, initiation, routine monitoring and close-out visits Preparation and submissions to Ethics Committees Assistance in site contract/payment management Requirements: University degree in medicine, pharmacy, nursing or life science Minimum 1-2 years of previous on-site monitoring experience in CRO or Pharma company Previous experience in preparation and submissions to Ethics Committees Thorough knowledge of ICH-GCP guidelines including an understanding of local regulatory requirements Fluent in local language and upper-intermediate English Availability to travel Computer literacy Driving license Strong organizational, communication and teamwork skills Ability to work independently and to effectively priorities tasks Company offers Competitive compensation and benefit program Salary rate is under discussion Medical insurance Mobile connection Car allowance, including fuel and parking compensation Opportunity to develop and grow
St Petersburg Russia
Clinical Research Associate (CRA) St Petersburg DOKUMEDS St Petersburg
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